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Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110
Recalled September 10, 2025 · FDA recall Z-2481-2025 · Medtronic Perfusion Systems
Hazard
The catheters may not retain their shape. · FDA Class I
Units
41200 units
Sold at
Worldwide - US Nationwide distribution.
Description
The catheters may not retain their shape.
Product
DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →